{"title":"Functionalized magnetic nanoprobe-based aptasensor for on-site detection of kanamycin in water by a personal glucose meter.","authors":"Ting Lei, Chengyan Yin, Hui Feng, Xiangwen Lei, Ruth Antwi-Baah, Jing Liu, Li Zhang, Wulin Yang, Shuxia Xu","doi":"10.1016/j.talanta.2025.128515","DOIUrl":null,"url":null,"abstract":"<p><p>In this work, the nanomagnetic probe was prepared by condensation of carboxylated kanamycin (Kana) aptamers with aminated nanomagnetic Fe<sub>3</sub>O<sub>4</sub> beads, which was coupled with invertase-labeled complementary DNA (cDNA) for sensitive and convenient detection of Kana in water samples by a personal glucose meter (PGM). In the absence of Kana, there was no PGM signal recorded because formed nanomagnetic probe was removed by magnetic separation. Conversely, the aptamer could recognize Kana specifically and released cDNA into supernatant. After the addition of sucrose, it was hydrolyzed into glucose by invertase. Detection of Kana was indirectly achieved based on the relationship between glucose concentration and the PGM indication. Furthermore, a miniaturized portable device was constructed by integrating the components using 3D printing technology. Under optimal conditions, rapid detection of Kana within the concentration range of 1-200 nM was achieved, with a detection limit (3σ/k) of 0.28 nM. Moreover, the proposed aptasensor was characterized in terms of selectivity, reproducibility and stability. Finally, it was applied to the determination of Kana in water with recoveries from 99% to 103%. All these results indicated that the proposed aptasensor is simple, rapid, selective, and sensitive, and it could potentially serve as an effective approach for the on-site determination of Kana in water samples.</p>","PeriodicalId":435,"journal":{"name":"Talanta","volume":"296 ","pages":"128515"},"PeriodicalIF":6.1000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Talanta","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.talanta.2025.128515","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/24 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
In this work, the nanomagnetic probe was prepared by condensation of carboxylated kanamycin (Kana) aptamers with aminated nanomagnetic Fe3O4 beads, which was coupled with invertase-labeled complementary DNA (cDNA) for sensitive and convenient detection of Kana in water samples by a personal glucose meter (PGM). In the absence of Kana, there was no PGM signal recorded because formed nanomagnetic probe was removed by magnetic separation. Conversely, the aptamer could recognize Kana specifically and released cDNA into supernatant. After the addition of sucrose, it was hydrolyzed into glucose by invertase. Detection of Kana was indirectly achieved based on the relationship between glucose concentration and the PGM indication. Furthermore, a miniaturized portable device was constructed by integrating the components using 3D printing technology. Under optimal conditions, rapid detection of Kana within the concentration range of 1-200 nM was achieved, with a detection limit (3σ/k) of 0.28 nM. Moreover, the proposed aptasensor was characterized in terms of selectivity, reproducibility and stability. Finally, it was applied to the determination of Kana in water with recoveries from 99% to 103%. All these results indicated that the proposed aptasensor is simple, rapid, selective, and sensitive, and it could potentially serve as an effective approach for the on-site determination of Kana in water samples.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.